KetoPASS: Observational Registry on Patients With Endogenous CS to Document Safety and Effectiveness of Ketoconazole.
Study Details
Study Description
Brief Summary
This is a non-interventional, prospective, multinational, multicentre, observational study, in which data collected are those derived from routine clinical practice via an European registry on CS: ERCUSYN.
| Condition or Disease | Intervention/Treatment | Phase |
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Detailed Description
The aim is to further document the safety and efficacy of Ketoconazole HRA administered in routine clinical practice in patients with CS.
The study operates under real clinical practice conditions, i.e. there is no treatment protocol thus.
Study Design
Outcome Measures
Primary Outcome Measures
- incidence of hepatotoxicity and QT prolongation to assess liver and cardiac tolerability profile of ketoconazole. [up to 5 years of follow up]
The primary objective is to document liver and cardiac tolerability profile of ketoconazole p.o when administered as monotherapy or in combination with other therapies, in routine clinical practice, in patients with CS.
Secondary Outcome Measures
- Number of patients with adverse events [up to 5 years of follow up]
Number of adverse events with Ketoconazole in monotherapy or in combination with other therapies for Cushing Syndrome.
- Drug utilization pattern regarding safe utilization of ketoconazole according to HRA SmPC recommendations on liver function [up to 5 years of follow up]
Number of liver tests performed per patient Number of patients for whom LFTs were performed according to SmPC recommendations. Number of patients with reduction of ketoconazole dose following liver enzymes increase Number of patients with interruptions / definitive stop of ketoconazole following liver enzymes increase
- Drug utilization pattern of ketoconazole according to HRA SmPC recommendations on liver function [up to 5 years of follow up]
Timing of liver tests performed per patient according to defined windows.
- Drug utilization pattern regarding safe use of ketoconazole according to HRA SmPC recommendations on liver function [up to 5 years of follow up]
Percentage of patients for whom LFTs were performed according to SmPC recommendations. Percentage of patients with reduction of ketoconazole dose following liver enzymes increase Percentage of patients with interruptions / definitive stop of ketoconazole following liver enzymes increase
- Drug utilization pattern regarding safe utilization of ketoconazole according to HRA SmPC recommendations on Qt interval monitoring. [up to 5 years of follow up]
Number of ECGs performed per patient Number of patients for whom ECGs were performed according to SmPC recommendations
- Drug utilization pattern of ketoconazole according to HRA SmPC recommendations on Qt interval monitoring. [up to 5 years of follow up]
Timing of ECGs performed per patient according to defined windows
- Drug utilization pattern regarding safe use of ketoconazole according to HRA SmPC recommendations on Qt interval monitoring. [up to 5 years of follow up]
Percentage of patients for whom ECGs were performed according to SmPC recommendations
- Effectiveness of ketoconazole [up to 5 years of follow up]
clinical outcome evaluated by the physician after ketoconazole treatment: cortisol levels improvement or normalization after ketoconazole treatment clinical symptoms of Cushing Syndrome over time. Number and type of comorbidities. Number of concomitant treatments for comorbidities by drug class.
- Impact on Quality of life, European Quality of Life questionnaire [up to 5 years of follow up]
self-administered questionnaire of Health-Related Quality of Life to evaluate current health regarding mobility, self-care, usual activities, pain/discomfort and anxiety/depression, and the perceived health status of the patient. The answers given can be converted into utility scores anchored at 0 for death and 1 for perfect health. The questionnaire also includes a Vi-sual Analog Scale (VAS), by which respondents can reporttheir perceived health status with a grade ranging from 0(the worst possible health status) to 100 (the best possiblehealth status).
- Impact on Quality of life, Cushing Quality of Life questionnaire [up to 5 years of follow up]
items referring to problems relevant to patients with CS with five categories of response. Answers are rated on a scale of 1-5, where '1' corresponds to 'Always' or 'Very much' and '5' to 'Never' or 'Not at all'. Therefore, the lower the score, the greater the impact on Health-Related Quality of Life.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Male or female patients aged from 12 years or older with a diagnosis of CS
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Patients who started ketoconazole therapy after study start
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For patients previously treated with ketoconazole, patients must have taken their last dose at least 6 months before starting ketoconazole again in this study.
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Written informed consent signed prior to registration of any patient data in HRA modules.
Exclusion Criteria:
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Adrenal cortical carcinoma
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Patients currently participating in any other trial (interventional or not) of an investigational medicine or participation in the past one month before start of ketoconazole
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Patients who have at least one contraindication among those listed in section 4.3 of the ketoconazole SmPC
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University Hospital Zagreb | Zagreb | Croatia | ||
| 2 | Hôpital Universitaire Grenoble | Grenoble | France | ||
| 3 | Hôpital Bicêtre APHP | Le Kremlin-Bicêtre | France | ||
| 4 | Hôpital de la Conception | Marseille | France | ||
| 5 | Institut de Recerca de la Santa Creu i Sant Pau | Barcelona | Spain | ||
| 6 | Sahlgrenska University Hospital | Gothenburg | Sweden |
Sponsors and Collaborators
- HRA Pharma
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- Keto PASS